Method for preparing super capacitor electrode material Ni doped CoP3/foam nickel

ABSTRACT

A method for preparing a supercapacitor electrode material Ni doped CoP3/Ni foam is provided, and the CoP3 is applied to the supercapacitor for the first time. The method belongs to a technical field of synthesis and preparation of supercapacitor materials. The present invention adopts a low-temperature phosphating process to prepare the Ni-doped CoP3/foamed nickel as the electrode material of the supercapacitor, so as to provide advantages such as simple synthesis process, easy control, low cost and high specific capacity. The supercapacitor electrode material Ni doped CoP3/Ni foam prepared by the present invention has a hierarchical structure and a large specific surface area, which is beneficial to shorten an ion transmission path, reduce an interface resistance between the electrode material and electrolyte, provide more active sites, and provide a higher specific capacity in alkaline electrolyte. The electrode material shows great potential in electrochemical energy storage.

CROSS REFERENCE OF RELATED APPLICATION

The present invention claims priority under 35 U.S.C. 119(a-d) to CN201910949326.1, filed Oct. 8, 2019.

BACKGROUND OF THE PRESENT INVENTION Field of Invention

The present invention relates to a technical field of transition metalphosphide preparation and its supercapacitor electrode material, andmore particularly to a preparation method and performance exploration ofa Ni doped CoP₃/Ni foam material applied to the supercapacitor.

Description of Related Arts

Increasingly serious environmental pollution and exhaustion of fossilfuels have accelerated demand for new energy, and prompted scientificresearchers from all over the world to continuously find and developeco-friendly and renewable new energy. Supercapacitors are attractivebecause of high power density. Furthermore, supercapacitors havesignificant advantages in cycle life, charge and discharge speed,temperature range, safety performance, etc., which have good applicationprospects. Supercapacitors are energy storage and conversion devicesthat accumulate charges through physical adsorption and desorption(electric double layer capacitance) or chemical Faraday reaction(pseudocapacitance). The electrode materials, as a core structure, aremostly carbon materials, metal oxides and conductive polymers, but suchmaterials have problems such as low theoretical specific capacity andpoor electrical conductivity. Therefore, it is urgent to develop a newelectrode material with high theoretical specific capacity and highelectrical conductivity.

As a typical transition metal phosphide. CoP₃ is also a skutteruditematerial which exhibits excellent thermoelectric properties at themiddle temperature range. CoP₃ is abundant, eco-friendly and cheap. Inaddition, it has metal characteristics, which provides higherconductivity and comparable high theoretical specific capacity.Conventionally, research emphasis is mainly put on metal-rich andsingle-phosphorus phase metal phosphides. The American ACS APPLIEDMATERIALS & INTERFACES (2016, Volume 8, Issue 6, Page 3892) reportedCo₂P nano rod-like and flower-like structures prepared by a thermaldecomposition method, wherein at a current density of 1 Ag⁻¹, the massspecific capacitances are 284 Fg⁻¹ and 416 Fg⁻¹, respectively. TheBritish Journal of Materials Chemistry A (2018, Issue 37, Page 17905)reported a NiCoP nanosheet prepared by a hydrothermal method and alow-temperature phosphating method, wherein at a current density of 1Ag⁻¹, the mass specific capacitance is 1206 Fg⁻¹. Since the syntheticmethods cannot provide sufficient active sites and cannot solve theproblem of charge transfer resistance, the above-mentioned Co₂P andNiCoP have lower supercapacitor performance, which hinders their furtherapplication. Based on this, there has been no research on dopedphosphorus-rich phase phosphide materials with high specific capacityand high conductivity.

SUMMARY OF THE PRESENT INVENTION

An object of the present invention is to provide a method for preparingan electrode material of a supercapacitor with simple synthesis process,easy control, low cost and high specific capacity, and to apply theelectrode material to the supercapacitor for the first time. In Ni dopedCoP₃/Ni foam prepared by the method is used in the supercapacitor,wherein/means that Ni doped CoP₃ is grown in situ on Ni foam by achemical method. The electrode material has a hierarchical structure anda large specific surface area, which is beneficial to shorten an iontransmission path, reduce an interface resistance between the electrodematerial and electrolyte, provide more active sites, and provide ahigher specific capacity in alkaline electrolyte. The electrode materialshows great potential in electrochemical energy storage.

Accordingly, in order to accomplish the above objects, the presentinvention provides a method for preparing a supercapacitor electrodematerial Ni-doped CoP₃/Ni foam, which uses transition metal salt cobaltchloride, nickel acetate and organic ligand 2-methylimidazole as rawmaterials, and uses absolute ethanol and deionized water as solvents.Sodium hypophosphite is a phosphorus source, and the Ni foam is aconductive substrate. The Ni-doped CoP₃/Ni foam is prepared bylow-temperature phosphating, wherein active sites, conductivity andspecific surface area of the electrode material are optimized byadjusting an amount of Ni for substituting part of Co.

A supercapacitor electrode material is formed by Ni doped CoP₃/Ni foam,wherein/indicates the Ni doped CoP₃ is grown in situ on the Ni foam by achemical method.

A method for preparing a supercapacitor electrode material Ni dopedCoP₃/Ni foam comprises steps of:

step 1: dissolving a raw material cobalt chloride CoCl₂.6H₂O indeionized water to form a solution with a molar concentration of0.04-0.06 M and dissolving a raw material 2-methylimidazole C₄H₆N₂ indeionized water to form a solution with a molar concentration of 0.3-0.5M: and dispersing the solutions by ultrasonic to form uniform solutions;then pouring the solution of 2-methylimidazole into the solution ofcobalt chloride, and ultrasonicating for 5-10 minutes; adding processedsponge-like Ni foam, wherein the Ni foam is ultrasonicated with ethanoland 6 M hydrochloric acid for 20 minutes, washed with deionized water tobe neutral and then dried at 50 degrees Celsius; the Ni foam has an areadensity of 280-420 g/m² and a pore diameter of 0.2-0.6 mm; afterreacting at 20-30 degrees Celsius for 6-12 hours, washing the Ni foamwith ionized water and absolute ethanol, and drying under vacuum at 60degrees Celsius for 12 hours to obtain Co-precursor/Ni foam;

step 2: placing the Co-precursor/Ni foam obtained in the step 1 inabsolute ethanol solution containing 0.005-0.02 M nickel acetate(C₄H₆O₄Ni.4H₂O) for 10-30 minutes, and washing with deionized water andabsolute ethanol; then drying under vacuum at 60 degrees Celsius for 12hours to obtain Ni-doped Co(OH)₂/Ni foam precursor; and

step 3: placing the Ni-doped Co(OH)₂/Ni foam precursor obtained in thestep 2 in a quartz boat, and placing the quartz boat at a downstream ofa tube furnace, placing 0.5-1.5 g sodium hypophosphite NaH₂PO₂ onanother quartz boat at an upstream; under nitrogen protection, setting afurnace temperature at 500-600 degrees Celsius and keeping for 1-2hours; after the furnace temperature is naturally cooled to a roomtemperature, washing with deionized water and absolute ethanol; thendrying under vacuum at 60 degrees Celsius for 12 hours to obtain theNi-doped CoP₃/Ni foam electrode material.

The present invention adopts a low-temperature phosphating process to 1o prepare the Ni-doped CoP₃/foamed nickel as the electrode material ofthe supercapacitor, so as to provide advantages such as simple synthesisprocess, easy control, low cost and high specific capacity. In addition,a hierarchical porous structure is conducive to rapid ion transfer andenhancing interaction with electrolyte, and is conducive to rapid andsufficient charge and discharge, thereby providing more specificcapacity and better rate performance.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is an X-ray diffraction pattern of a supercapacitor electrodematerial Ni-doped CoP₃/Ni foam obtained in embodiment 2; wherein X-raydiffraction characteristic peaks are well matched with standard cardsCoP₃ JCPDS (24-0496) and Ni JCPDS (70-0989); because an amount ofincorporated Ni is low, only characteristics diffraction peaks of the Nifoam and the CoP₃ appear on spectrum, which proves that samples preparedin the embodiment 2 are indeed Ni-doped CoP₃/Ni foam supercapacitorelectrode materials;

FIG. 2 is cyclic voltammetry curves of the supercapacitor electrodematerial Ni-doped CoP₃/Ni foam obtained in the embodiment 2 at differentscanning speed rates;

FIG. 3 is constant current charging and discharging curves of thesupercapacitor electrode material Ni-doped CoP₃/Ni foam obtained in theembodiment 2 at different current densities:

FIG. 4 illustrates a specific capacitance retention rate of thesupercapacitor electrode material Ni-doped CoP₃/Ni foam obtained in theembodiment 2 after 10,000 cycles of charging and discharging at acurrent density of 10 mA cm⁻²:

FIG. 5 illustrates specific capacities of supercapacitor electrodematerials Ni-doped CoP₃/Ni foam obtained in embodiments 1-4 at differentcurrent densities.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

Referring to the drawings, embodiments of the present invention will befurther illustrated.

Embodiment 1

A method for preparing a supercapacitor electrode material Ni dopedCoP₃/Ni foam comprises steps of:

step 1: respectively dissolving 0.476 g cobalt chloride CoCl₂.6H₂O and1.312 g 2-methylimidazole C₄H₆N₂ in 40 ml deionized water, anddispersing the solutions by ultrasonic to form uniform solutions; thenpouring the solution of 2-methylimidazole into the solution of cobaltchloride, and ultrasonicating for 5-10 minutes; adding processedsponge-like Ni foam, wherein the Ni foam is ultrasonicated with ethanoland 6 M hydrochloric acid for 20 minutes, washed with deionized water tobe neutral and then dried at 50 degrees Celsius; selecting Ni foam withan area density of 280, 400 and 420 g/m² and a pore diameter of 0.2, 0.4and 0.6 mm for studying impacts thereof on the supercapacitor; afterreacting at 25 degrees Celsius for 12 hours, washing the Ni foam withionized water and absolute ethanol, and drying under vacuum at 60degrees Celsius for 12 hours to obtain Co-precursor/Ni foam:

step 2: placing the Co-precursor/Ni foam obtained in the step 1 in 40 mlabsolute ethanol solution containing 48 mg nickel acetate(C₄H₆O₄Ni.4H₂O) for 20 minutes, and washing with deionized water andabsolute ethanol; then drying under vacuum at 60 degrees Celsius for 12hours to obtain Ni-doped Co(OH)₂/Ni foam precursor; and

step 3: placing the Ni-doped Co(OH)₂/Ni foam precursor obtained in thestep 2 in a quartz boat, and placing the quartz boat at a downstream ofa tube furnace; placing 0.5-1.5 g sodium hypophosphite NaH₂PO₂ onanother quartz boat at an upstream; under nitrogen protection, setting afurnace temperature at 500 degrees Celsius and keeping for 2 hours;after the furnace temperature is naturally cooled to a room temperature,washing with deionized water and absolute ethanol; then drying undervacuum at 60 degrees Celsius for 12 hours to obtain the Ni-doped CoP₃/Nifoam electrode material.

Embodiment 2

step 1: respectively dissolving 0.476 g cobalt chloride CoCl₂.6H₂O and1.312 g 2-methylimidazole C₄H₆N₂ in 40 ml deionized water, anddispersing the solutions by ultrasonic to form uniform solutions: thenpouring the solution of 2-methylimidazole into the solution of cobaltchloride, and ultrasonicating for 5-10 minutes: adding processedsponge-like Ni foam, wherein the Ni foam is ultrasonicated with ethanoland 6 M hydrochloric acid for 20 minutes, washed with deionized water tobe neutral and then dried at 50 degrees Celsius: selecting Ni foam withan area density of 280, 400 and 420 g/m² and a pore diameter of 0.2, 0.4and 0.6 mm for studying impacts thereof on the supercapacitor; afterreacting at 25 degrees Celsius for 12 hours, washing the Ni foam withionized water and absolute ethanol, and drying under vacuum at 60degrees Celsius for 12 hours to obtain Co-precursor/Ni foam;

step 2: placing the Co-precursor/Ni foam obtained in the step 1 in 40 mlabsolute ethanol solution containing 96 mg nickel acetate(C₄H₆O₄Ni.4H₂O) for 20 minutes, and washing with deionized water andabsolute ethanol; then drying under vacuum at 60 degrees Celsius for 12hours to obtain Ni-doped Co(OH)₂/Ni foam precursor: and

step 3: placing the Ni-doped Co(OH)₂/Ni foam precursor obtained in thestep 2 in a quartz boat, and placing the quartz boat at a downstream ofa tube furnace, placing 0.5-1.5 g sodium hypophosphite NaH₂PO₂ onanother quartz boat at an upstream; under nitrogen protection, setting afurnace temperature at 500 degrees Celsius and keeping for 2 hours;after the furnace temperature is naturally cooled to a room temperature,washing with deionized water and absolute ethanol; then drying undervacuum at 60 degrees Celsius for 12 hours to obtain the Ni-doped CoP₃/Nifoam electrode material.

The Ni-doped CoP₃/Ni foam electrode material prepared in the embodiment2 is used as a working electrode, a platinum sheet is used as anauxiliary electrode, and a HgO/Hg electrode is used as a referenceelectrode, which are all immersed in 6 M KOH electrolyte to form athree-electrode system. A supercapacitor performance test is performedat a potential window of 0-0.6V. FIG. 2 is cyclic voltammetry curves ofthe Ni-doped CoP₃/Ni foam electrode material at different scanning speedrates. All curves have obvious redox peaks, indicating pseudocapacitancecharacteristics of such material. The curves maintain relativelyconsistent shapes from 2 mV s⁻¹ to 15 mV s⁻¹, showing rapid redoxreaction. FIG. 3 is test curves of charge and discharge properties atdifferent current densities, wherein all the test curves have dischargeplatforms, indicating redox capacitance characteristics. When thecurrent density is 2.5 mA cm⁻², an area specific capacitance is 5.1 Fcm⁻² (a corresponding mass specific capacitance is 2780 F g⁻¹). At thistime, the area density of the Ni foam used is 400 g/m², and the porediameter is 0.6 mm. When the current density is increased to 40 mA cm⁻²,the area specific capacitance is still 3.4 F cm⁻², showing sufficientrate performance. FIG. 4 shows that the specific capacitance retentionrate of the electrode material remains above 90% after 10,000 cycles ofcontinuous charging and discharging at a scanning speed rate of 10 mAcm⁻², indicating great advantage as the supercapacitor electrodematerial.

Embodiment 3

step 1: respectively dissolving 0.476 g cobalt chloride CoCl₂.6H₂O and1.312 g 2-methylimidazole C₄H₆N₂ in 40 ml deionized water, anddispersing the solutions by ultrasonic to form uniform solutions; thenpouring the solution of 2-methylimidazole into the solution of cobaltchloride, and ultrasonicating for 5-10 minutes; adding processedsponge-like Ni foam, wherein the Ni foam is ultrasonicated with ethanoland 6 M hydrochloric acid for 20 minutes, washed with deionized water tobe neutral and then dried at 50 degrees Celsius; selecting Ni foam withan area density of 280, 400 and 420 g/m² and a pore diameter of 0.2, 0.4and 0.6 mm for studying impacts thereof on the supercapacitor; afterreacting at 25 degrees Celsius for 12 hours, washing the Ni foam withionized water and absolute ethanol, and drying under vacuum at 60degrees Celsius for 12 hours to obtain Co-precursor/Ni foam;

step 2: placing the Co-precursor/Ni foam obtained in the step 1 in 40 mlabsolute ethanol solution containing 144 mg nickel acetate(C₄H₆O₄Ni.4H₂O) for 20 minutes, and washing with deionized water andabsolute ethanol; then drying under vacuum at 60 degrees Celsius for 12hours to obtain Ni-doped Co(OH)₂/Ni foam precursor; and

step 3: placing the Ni-doped Co(OH)₂/Ni foam precursor obtained in thestep 2 in a quartz boat, and placing the quartz boat at a downstream ofa tube furnace, placing 0.5-1.5 g sodium hypophosphite NaH₂PO₂ onanother quartz boat at an upstream: under nitrogen protection, setting afurnace temperature at 500 degrees Celsius and keeping for 2 hours;after the furnace temperature is naturally cooled to a room temperature,washing with deionized water and absolute ethanol; then drying undervacuum at 60 degrees Celsius for 12 hours to obtain the Ni-doped CoP₃/Nifoam electrode material.

Embodiment 4

step 1: respectively dissolving 0.476 g cobalt chloride CoCl₂.6H₂O and1.312 g 2-methylimidazole C₄H₆N₂ in 40 ml deionized water, anddispersing the solutions by ultrasonic to form uniform solutions; thenpouring the solution of 2-methylimidazole into the solution of cobaltchloride, and ultrasonicating for 5-10 minutes; adding processedsponge-like Ni foam, wherein the Ni foam is ultrasonicated with ethanoland 6 M hydrochloric acid for 20 minutes, washed with deionized water tobe neutral and then dried at 50 degrees Celsius; selecting Ni foam withan area density of 280, 400 and 420 g/m² and a pore diameter of 0.2, 0.4and 0.6 mm for studying impacts thereof on the supercapacitor: afterreacting at 25 degrees Celsius for 12 hours, washing the Ni foam withionized water and absolute ethanol, and drying under vacuum at 60degrees Celsius for 12 hours to obtain Co-precursor/Ni foam:

step 2: placing the Co-precursor/Ni foam obtained in the step 1 in 40 mlabsolute ethanol solution containing 192 mg nickel acetate(C₄H₆O₄Ni.4H₂O) for 20 minutes, and washing with deionized water andabsolute ethanol; then drying under vacuum at 60 degrees Celsius for 12hours to obtain Ni-doped Co(OH)/Ni foam precursor: and

step 3: placing the Ni-doped Co(OH)₂/Ni foam precursor obtained in thestep 2 in a quartz boat, and placing the quartz boat at a downstream ofa tube furnace; placing 0.5-1.5 g sodium hypophosphite NaH₂PO₂ onanother quartz boat at an upstream; under nitrogen protection, setting afurnace temperature at 500 degrees Celsius and keeping for 2 hours:after the furnace temperature is naturally cooled to a room temperature,washing with deionized water and absolute ethanol; then drying undervacuum at 60 degrees Celsius for 12 hours to obtain the Ni-doped CoP₃/Nifoam electrode material.

XRD and supercapacitor performance tests are performed on the Ni-dopedCoP₃/Ni foam material prepared in the embodiments 1-4. Results are shownin FIGS. 1-5.

FIG. 1 is an X-ray diffraction pattern of a supercapacitor electrodematerial Ni-doped CoP₃/Ni foam obtained in embodiment 2; wherein X-raydiffraction characteristic peaks are well matched with standard cardsCoP₃ JCPDS (24-0496) and Ni JCPDS (70-0989); because an amount ofincorporated Ni is low, only characteristics diffraction peaks of the Nifoam and the CoP₃ appear on spectrum, which proves that samples preparedin the embodiment 2 are indeed Ni-doped CoP₃/Ni foam supercapacitorelectrode materials.

FIG. 2 is cyclic voltammetry curves of the Ni-doped CoP₃/Ni foamelectrode material prepared in the embodiment 2 at different scanningspeed rates. All curves have obvious redox peaks, indicatingpseudocapacitance characteristics of such material. The curves maintainrelatively consistent shapes from 2 mV s⁻¹ to 15 mV s⁻¹, showing rapidredox reaction. FIG. 3 is test curves of charge and discharge propertiesof the Ni-doped CoP₃/Ni foam electrode material prepared in theembodiment 2 at different current densities (2.5 mA cm⁻², 5 mA cm⁻², 10mA cm⁻², 20 mA cm⁻² and 40 mA cm⁻²), wherein all the test curves havedischarge platforms, further indicating redox capacitancecharacteristics. When the current density is 2.5 mA cm⁻², an areaspecific capacitance is 5.1 F cm⁻² (a corresponding mass specificcapacitance is 2780 F g⁻¹). At this time, the area density of the Nifoam used is 400 g/m², and the pore diameter is 0.6 mm. When the currentdensity is increased to 40 mA cm⁻², the area specific capacitance isstill 3.4 F cm⁻², showing sufficient rate performance. FIG. 4 shows thatthe specific capacitance retention rate of the electrode materialremains above 90% after 10.000 cycles of continuous charging anddischarging when a current density of the Ni-doped CoP₃/Ni foamelectrode material prepared in the embodiment 2 is 10 mA cm⁻²,indicating great advantage as the supercapacitor electrode material.FIG. 5 illustrates specific capacities of the Ni-doped CoP₃/Ni foamelectrode materials obtained in embodiments 1-4 at current densities of2.5 mA cm⁻². 5 mA cm⁻², 10 mA cm⁻², 20 mA cm⁻² and 40 mA cm⁻². Referringto the drawings, the Ni-doped CoP₃/Ni foam electrode material obtainedin the embodiment 2 has the largest specific capacity at each currentdensity. The Ni-doped CoP₃/Ni foam electrode materials prepared by thepresent invention have excellent supercapacitor performance, and thesample prepared in the embodiment 2 has the best performance.

What is claimed is:
 1. A supercapacitor electrode material, formed by Nidoped CoP₃/Ni foam, wherein/indicates the Ni doped CoP₃ is grown in situon the Ni foam by a chemical method.
 2. A method for preparing asupercapacitor electrode material Ni doped CoP₃/Ni foam, comprisingsteps of: step 1: dissolving a raw material cobalt chloride CoCl₂.6H₂Oin deionized water to form a solution with a molar concentration of0.04-0.06 M and dissolving a raw material 2-methylimidazole C₄H₆N₂ indeionized water to form a solution with a molar concentration of 0.3-0.5M; and dispersing the solutions by ultrasonic to form uniform solutions;then pouring the solution of 2-methylimidazole into the solution ofcobalt chloride, and ultrasonicating for 5-10 minutes; adding processedsponge-like Ni foam, wherein the Ni foam is ultrasonicated with ethanoland 6 M hydrochloric acid for 20 minutes, washed with deionized water tobe neutral and then dried at 50 degrees Celsius; the Ni foam has an areadensity of 280-420 g/m² and a pore diameter of 0.2-0.6 mm; afterreacting at 20-30 degrees Celsius for 6-12 hours, washing the Ni foamwith ionized water and absolute ethanol, and drying under vacuum at 60degrees Celsius for 12 hours to obtain Co-precursor/Ni foam; step 2:placing the Co-precursor/Ni foam obtained in the step 1 in absoluteethanol solution containing 0.005-0.02 M nickel acetate (C₄H₆O₄Ni.4H₂O)for 10-30 minutes, and washing with deionized water and absoluteethanol; then drying under vacuum at 60 degrees Celsius for 12 hours toobtain Ni-doped Co(OH)₂/Ni foam precursor; and step 3: placing theNi-doped Co(OH)₂/Ni foam precursor obtained in the step 2 in a quartzboat, and placing the quartz boat at a downstream of a tube furnace;placing 0.5-1.5 g sodium hypophosphite NaH₂PO₂ on another quartz boat atan upstream; under nitrogen protection, setting a furnace temperature at500-600 degrees Celsius and keeping for 1-2 hours; after the furnacetemperature is naturally cooled to a room temperature, washing withdeionized water and absolute ethanol; then drying under vacuum at 60degrees Celsius for 12 hours to obtain the Ni-doped CoP₃/Ni foamelectrode material.